Canonical Allele Identifier: CA734642584
Gene: TTC34 HGNC NCBI

Linked Data

dbSNP Id: rs1447333555
MyVariant Identifiers: chr1:g.2709190C>G (hg19) chr1:g.2792625C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2792625C>G , CM000663.2:g.2792625C>G GRCh38
NC_000001.10:g.2709190C>G , CM000663.1:g.2709190C>G GRCh37
NC_000001.9:g.2699050C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401095.9:c.785-2279G>C MANE Select ENSP00000383873.4:n.785-2279G>C
ENST00000401095.8:c.785-2279G>C ENSP00000383873.4:n.785-2279G>C
NM_001242672.2:c.785-2279G>C NP_001229601.2:n.785-2279G>C
NM_001242672.3:c.785-2279G>C MANE Select NP_001229601.2:n.785-2279G>C
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